Across TCGA pan-cancer cohorts, IGHV3-33 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IGHV3-33 data layer compared with 23 for mass-spec protein.
The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher IGHV3-33 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHV3-33 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
DLBC, GBM, and SKCM are the cancer types where IGHV3-33 Mutation most reproducibly stratifies survival.